MSK Diagnosis Flashcards
Spinal stenosis?
MRI
Ankylosing spondylitis?
Labs: Increased ESR and Negative RA and ANA.
Xray: Bamboo Spine and Sacroilitis.
Herniated disc?
Definitive Diagnosis: MRI.
Xray shows loss of disc height.
Compression fracture?
Xray: Loss of vertebral height.
MRI or CT if neuro symptoms.
Spondylolysis?
Lateral xray: radiolucent defect in pars; oblique: “scotty dog” w/ collar which shows a break in the pars interarticularis.
CT
Bone scan.
Spondylothisthesis?
Xray: Forward slipping on vertebra. Lateral views to measure slip angle and grade; flex/extension views can help eval stability.
MRI if neuro symptoms.
RA?
Labs: RF and ACPA + and elevated ESR and C-reactive protein.
Xray: Loss of junta articular bone mass. Narrowing of joint space. Boney erosions at margins of joint.
RA diagnosis criteria?
Inflammatory arthritis of three or more joints
Symptoms lasting at least 6 weeks
Elevated CRP and ESR
Positive serum RF or ACPA
Radiographic changes consistent with RA (erosions and periarticular decalcification)
Reactive arthritis/Reiter Syndrome?
Synovial fluid for analysis.
Polyarteritis nodosa?
Increased ESR, proteinuria. ANCA -. Renal and mesenteric angiography: microaneurysms “beading”/strung together “rosary sign”.
Definitive: Biopsy shows necrotizing medium vessel vasculitis & no granulomas.
Polymyalgia rheumatica?
ESR elevated. Normal CK and aldolase.
Polymyositis and Dermatomyositis?
Best Initial: Elevated CK and Aldolase. \+ anti JO 1 and ANA. Increased ESR & CRP, RF. Definitive Diagnosis: Muscle biopsy Abnml EMG.
Fibromyalgia?
Multiple trigger points. Symmetrical.
Criteria:
1. Widespread pain including axial pain for at least 3 months.
2. Pain in at least 11/18 tender point sites.
Sjogren Syndrome?
Best Initial: ANA + & AntiSS-A and -B.
Schirmer test: decreased tear production (wetting of < 5mm
of the filter paper placed in the lower eyelid for 5 minutes.
Definitive: salivary gland (lip or parotid) biopsy
Scleroderma?
Anti-centromere antibodies.
Anti-SCL-70 antibodies - associated with diffuse disease & multiple organ involvement.
ANA+.
Lupus?
Positive ANA.
Anti-double stranded DNA and anti-Smith antibodies - the presence of either is diagnostic of SLE.
Antiphospholipid antibodies = increased risk of arterial & venous thrombosis.
Pancytopenia: anemia of chronic disease, leukopenia, lymphopenia, thrombocytopenia.
Decreased compliment levels (C3, C4).
Antiphospholipid syndrome?
Anticardiolipin antibodies; lupus anticoagulant = increased PTT.
Juvenile (Idiopathic) RA?
Clinical, but with increased ESR, CRP; positive ANA if oligoarticular; 15% are RF positive. Still’s is often associated with negative RF and ANA.
Pelvic Fracture?
X-ray
Hip dislocation?
X-ray of pelvis and hip.
CT scan to further evaluate associated fractures.
Hip fracture?
X-ray.
Trochanteric bursitis?
Clinical as x-rays are unremarkable.
Slipped capital femoral epiphysis (SCFE)?
X-ray- frog leg or lateral (posterior displacement of femoral epiphysis - ICE CREAM fell off the cone).
Legg-Calve-Perthes Disease?
Early: Increased density of femoral epiphysis, widening of cartilage space.
Advanced: Deformity, + crescent sign (microfractures w/ collapse of bone)
Femoral Shaft fracture?
X-ray.
Tibial and fibular fractures?
X-ray.
Popliteal (Baker’s) Cyst?
Doppler to r/o DVT and identifies cyst.
LCL and MCL?
MRI.
ACL PE?
Lachman Test=Most sensitive.
Pivot Shift Test.
Anterior Drawer Test.
ACL?
X-ray to r/o fracture.
MRI.
PCL?
MRI.
Meniscal tear PE?
Positive McMurray sign = pop/click
Apley test with joint line tenderness, effusion, swelling.